- Research article
- Open Access
Expressions of ECE-CYC2 clade genes relating to abortion of both dorsal and ventral stamens in Opithandra(Gesneriaceae)
© Song et al; licensee BioMed Central Ltd. 2009
- Received: 13 April 2009
- Accepted: 7 October 2009
- Published: 7 October 2009
ECE-CYC2 clade genes known in patterning floral dorsoventral asymmetry (zygomorphy) in Antirrhinum majus are conserved in the dorsal identity function including arresting the dorsal stamen. However, it remains uncertain whether the same mechanism underlies abortion of the ventral stamens, an important morphological trait related to evolution and diversification of zygomorphy in Lamiales sensu lato, a major clade of predominantly zygomorphically flowered angiosperms. Opithandra (Gesneriaceae) is of particular interests in addressing this question as it is in the base of Lamiales s.l., an early representative of this type zygomorphy.
We investigated the expression patterns of four ECE-CYC2 clade genes and two putative target cyclinD3 genes in Opithandra using RNA in situ hybridization and RT-PCR. OpdCYC gene expressions were correlated with abortion of both dorsal and ventral stamens in Opithandra, strengthened by the negatively correlated expression of their putative target OpdcyclinD3 genes. The complement of OpdcyclinD3 to OpdCYC expressions further indicated that OpdCYC expressions were related to the dorsal and ventral stamen abortion through negative effects on OpdcyclinD3 genes.
These results suggest that ECE-CYC2 clade TCP genes are not only functionally conserved in the dorsal stamen repression, but also involved in arresting ventral stamens, a genetic mechanism underlying the establishment of zygomorphy with abortion of both the dorsal and ventral stamens evolved in angiosperms, especially within Lamiales s.l.
- Dorsal Region
- Floral Tissue
- Stamen Primordia
- Stamen Development
- Fertile Stamen
One important event during the evolution of angiosperms is the emergence of flower bilateral symmetry, i.e. zygomorphy, a key innovation associated with important adaptive radiations . Several zygomorphic clades have independently evolved successfully from actinomorphic ancestors in angiosperms, including Lamiales sensu lato that includes a major genetic model organism snapdragon (Antirrhinum majus) [2, 3].
In A.majus, CYCLOIDEA (CYC) and DICHOTOMA (DICH) are essential for the development of dorsoventral asymmetry in flowers due to their dorsal identity function, i.e. controlling the fate of the dorsal floral organs in the second and third whorls [4, 5]. CYC promotes cell expansion in the dorsal petals, while it arrests the growth of the dorsal stamen to become a staminode [4, 5]. Meanwhile, DICH activity affects the internal asymmetry of the dorsal petals [4, 5]. The ability of CYC to arrest the dorsal stamen depends on its negative effect on expression of cell-cycle genes, such as cyclin D3b [3, 6]. CYC and DICH encode proteins within the ECE-CYC2 clade (ECE lineage, CYC/TB1 subfamily) in the TCP family of transcription factors with TCP domain related to cell proliferation [3, 7–12]. In legumes, distantly related to A. majus, several CYC homologues, such as LjCYC2 in Lotus and PsCYC2 in pea, also have the function in establishing dorsal identity in legume flowers [13, 14]. In Arabidopsis thaliana, a model eudicot species with ancestrally actinomorphic flowers, and its close relative Iberis amara, CYC homologues, TCP1 and IaTCP1 genes are characteristic of dorsal identity function, in which IaTCP1 dorsal-specific expression represses the two dorsal petal development in Iberis amara [15, 16]. Recent studies in the sunflower family (Asteraceae) show that CYC-like genes, i.e. RAY1, RAY2 in Senecio and GhCYC2 in Gerbera, have played a key role in the establishment and evolution of the capitulate inflorescence [17, 18]. Therefore, it is suggested that CYC-like TCP genes have been recruited multiple times for a role of dorsal identity and its modifications in establishing zygomorphy in core eudicots [3, 19]. Even though the genetic control for the floral dorsoventral asymmetry has been intensively studied in model systems, it is still a great challenge to explain how modifications of development led to the transformation among different types of zygomorphy and the morphological diversification of zygomorphy in angiosperms, especially in Lamiales s.l., a major clade of predominantly zygomorphically flowered angiosperms.
Zygomorphy is believed to be ancestral in Lamiales s.l. [2, 19, 20]. Most zygomorphic groups in Lamiales s.l. have a pentamerous perianth with four stamens plus a dorsal staminode and two carpels as in A.majus. However, there is a great variation in morphology and number of corolla lobes and stamens . The dorsal staminode can be completely lost as in Rehmannia and Veronica (Scrophulariaceae sensu lato) [2, 21, 22] and the two lateral stamens may become aborted instead of one dorsal staminode as in Mohavea (Scrophulariaceae s.l.) and Chirita (Gesneriaceae) [23–25]. In some cases, the two ventral stamens may become staminodes rather than the lateral stamens and the dorsal one, such as in Opithandra and Epithema (Gesneriaceae) . In extreme cases, each flower may have only a single stamen as in Hippuris (Scrophulariaceae s.l.) . In Mohavea, a close relative of A. majus, there is a derived floral morphology with abortion of both the dorsal and lateral stamens unlike the flowers of A.majus with abortion of only the dorsal stamen . The derived floral morphology of Mohavea is correlated with the expression changes of McCYC/McDICH via CYC/DICH, i.e. expansion from the dorsal to both the dorsal and lateral stamens . A similar correlation of expanded expression of CYC-like genes with abortion of both the dorsal and lateral stamens is also observed in Chirita (Gesneriaceae) . However, we are still not clear about the abortion of the ventral stamens that has been involved in the evolutionary shifts of stamen number during the morphological diversification of zygomorphy in Lamiales s.l. .
In addition, in the backpetals mutant in A.majus, the ectopic expression of CYC in the lateral and ventral positions results in a dorsalized corolla. However, it seems likely that the androecial development is not affected by the ectopic expression of CYC because the two lateral and two ventral stamens are still fertile [5, 26]. In the actinomorphic flower of legume Cadia, no LegCYC1B mRNA is detected in stamens . It is hard to determine whether LegCYC1B or other CYC homologues in legumes have a role in controlling androecial development from data to date [13, 14, 21]. RAY2 in Senecio and GhCYC2 in Gerbera (Asteraceae) mainly promote the growth of the ligule (the ventral petals) in ray florets and are excluded from the dorsal rudimentary petals [17, 18]. In Veronica and Gratiola (Scrophulariaceae s.l.), some of CYC-like genes have dorsal-specific expressions while some have lost this feature, but their expressions do not correlate with ventral stamen arrest . Therefore, expression data correlated with the ventral stamen abortion have not been reported yet for members of the ECE-CYC2 clade. It is uncertain whether abortion of the ventral stamens is related to CYC-like gene activities or to the effect of an unknown analogous counterpart of CYC-like genes, such as members of ECE-CYC3 clade or other factors [3, 12, 20].
Here we report that there is a correlation between OpdCYC gene expressions and abortion of both the dorsal and ventral stamens in Opithandra, strengthened by the negatively correlated expression of their putative direct target OpdcyclinD3 genes. The novel patterns of CYC-like gene expressions in Opithandra indicate that ECE-CYC2 clade TCP genes are involved in the ventral stamen repression evolved within Lamiales s. l..
Sequence and phylogenetic analyses of OpdCYC and OpdcyclinD3
Two D3-type cyclin genes, designated as OpdcyclinD3a and OpdcyclinD3b, were isolated from O. dinghushanensis with full length ORFs of 1563 bp and 1200 bp, respectively (Additional file 1B). The two D3-type cyclin genes contain a cyclin box  and the putative (Rb)-binding motif (LxCxE, where x is any amino acid) which are found both in animals [30, 31] and plants [6, 32, 33]. Phylogenetic analyses show that OpdcyclinD3 genes belong to cyclinD3a and cyclinD3b clade, respectively, in the cyclinD3 lineages, in which they have close relations with AmcyclinD3a and AmcyclinD3b from A.majus, respectively (Figure 2C).
Gene mRNA expression patterns
In contrast to OpdCYC1C, OpdCYC2A mRNA densely accumulated in the dorsal region of the floral apex as petals and stamens became visible (Figure 3H). Then, the OpdCYC2A expression signal was specifically concentrated in the dorsal petals and the dorsal staminode (Figure 3I-J). As floral organs developed, OpdCYC2A transcripts continued to be highly concentrated at the dorsal staminode and the dorsal-most parts of the two dorsal petals (Figure 3J-K). In the middle stages, the strong mRNA signal of OpdCYC2A was detected in the dorsal region (the dorsal petals and staminode) shown in RT-PCR that declined in late stages with no signal in other regions (Figure 4A-B, D). Its mRNA was undetectable in stamens as pollen sacs began development in the two lateral anthers while the two ventral anthers became sterile (Figure 3L). Even though OpdCYC1D expression was undetectable in floral tissues using in situ hybridization (Figure 3M), its very weak mRNA signals were detected in the dorsal region (the dorsal petals and staminode) from middle to late stages using RT-PCR (Figure 4A-B). OpdCYC2B mRNA was not detectable in floral tissues both using in situ hybridization and RT-PCR (Figure 3N, Figure 4A-B). No signal was detected in floral tissues with sense probes of OpdCYC1C (Figure 3O) and OpdCYC2A (Figure 3P).
To further elucidate the role of OpdCYC genes in floral development of Opithandra dinghushanensis, we carried out semiquantitative RT-PCR studies of two OpdcyclinD3 genes because cyclinD3 genes were previously revealed to be negatively controlled by CYC as shown in the mid-to-late stage flowers in the model organism snapdragon . RT-PCR results showed that OpdcyclinD3a was strongly expressed in lateral stamens from middle to late stages while its weak mRNA signal was also detected in lateral and ventral petals (Figure 4A-B, E). OpdcyclinD3a mRNA was not detected either in the dorsal region (the dorsal petals and staminode) and ventral staminodes (Figure 4A-B, E). OpdcyclinD3b transcripts were widely distributed in floral tissues except ventral staminodes, in which its mRNA signal was strong in lateral stamens from middle to late stages (Figure 4A-B, F). Transcripts of OpdcyclinD3b detected in the dorsal region were likely mainly distributed in the dorsal petals (OpdcyclinD3b mRNA was uneasily detectable in the dorsal staminode using in situ hybridization (data not shown)).
The androecium of Opithandra only has two fertile stamens at the lateral positions with three sterile stamens (staminodes) at the dorsal and ventral sides (Figure 1) (also see ). The dorsal aborted stamen is tiny and barely detectable at anthesis while the two infertile ventral stamens have short filaments with very small and sterile anthers (Figure 1B-C). Correlative with the differentiation along the dorsoventral axis of the morphologically peculiar androecium, the OpdCYC2A strong expression is restricted to the dorsal staminode while OpdCYC1C transcripts are initially distributed in all five stamen primordia but later are concentrated in the dorsal and ventral staminodes to late stages. In the ECE lineage of CYC/TB1 subfamily, the TCP proteins in ECE-CYC2 clade studied to date function as negative regulators in stamen development, whereas they appear to vary in petal development according to the trait concerned [3–5, 9, 10, 12, 17, 23, 25, 34, 35]. The abortion of the dorsal stamen in Antirrhinum comes from CYC and DICH activities [4, 5]. The CYC-like gene expression expansion from the dorsal to both the dorsal and lateral stamens is correlated with abortion of both the dorsal and lateral stamens in Mohavea and Chirita [23, 25]. TB1 gene exhibits a mix feature of ECE-CYC1 and ECE-CYC2 clades and functions to suppress axillary meristem (CYC1) while retard stamen growth (CYC2) in maize [3, 12, 34]. In Asteraceae, a CYC homologue GhCYC2 from Gerbera functions by disrupting stamen development . Given that CYC-like gene (ECE-CYC2 clade) function is conserved in repressing stamen development, OpdCYC2A expression restricted to the dorsal stamen and OpdCYC1C expression later concentrated in the dorsal and ventral stamens in the third whorl might be related to abortion of the dorsal and ventral stamens in Opithandra. In fact, the successive sections from the same individual flower indicate that correlative with OpdCYC gene strong expression, the early primordial growth have already been retarded in the dorsal and ventral staminodes in comparison with that in the lateral stamens.
Evidence shows that CYC functions to repress stamen development in the third whorl through its negative effect on expression of D3-type cyclin genes, including cyclinD3b, which usually play an important role in locally regulating cell proliferation in floral development [3, 6, 36]. The negative effects on cell cycle progression have been reported from other TCP genes, such as IaTCP1 from Iberis (Brassicaceae), TCP2 and TCP4 from Arabidopsis, and CIN from Antirrhinum [16, 37, 38]. We, therefore, investigated the expression pattern of OpdcyclinD3a and D3b to test for further correlation between CYC expression and stamen abortion through cell-cycle regulation, especially the ventral stamens. In strengthening the above suggestion, OpdcyclinD3 genes have expression patterns in floral tissues negatively correlated with those of OpdCYC genes and stamen abortion in Opithandra. Both Opdcyclin D3a and D3b transcripts are not detected, or weakly detected (i.e. dorsal), in the dorsal and ventral staminodes where both OpdCYC2A and OpdCYC1C or OpdCYC1C are strongly and continuously expressed throughout floral development, while their transcripts are much more concentrated in the lateral stamens where there is only a weak expression of OpdCYC1C in early stages. These factors indicate that OpdCYC gene activities may suppress the development of the dorsal and ventral stamens through negatively regulating OpdcyclinD3 genes (Figure 5). Our recent findings of consensus-binding sites of the TCP transcription factor in the 5' upstream regions of OpdcyclinD3 homologues, i.e. ChcyclinD3a and D3b in Chirita heterotricha, further support the direct regulatory relation between CYC-like and cyclinD3 genes in Gesneriaceae (Yang, Xia and Wang, Yin-Zheng, unpublished).
Zygomorphic flowers with three staminodes at the dorsal and lateral positions or at the dorsal and ventral sides have been considered to be derived in the family Gesneriaceae [24, 40–42]. In the primitive zygomorphic taxa, such as Haberlea and Oreocharis characteristic of tetrandrous flowers with four didynamous stamens plus a dorsal staminode, and the derived actinomorphic groups (definition see note in ), such as Ramonda and Bournea, there is only one single copy of GCYC1 and GCYC2, respectively, found to date (Figure 2B) [35, 39, 43, 44]. However, two copies of GCYC1 are frequently found in the advanced zygomorphic taxa, especially in the zygomorphic genera characterized by diandrous flowers with three staminodes, such as two African genera Streptocarpus and Saintpaulia with GCYC1A and GCYC1B [44, 45] and Asian genera Didymocarpus, Chirita and Loxostigma with GCYC1C and GCYC1D [25, 46] as well as Opithandra herein (Figure 2B). Recent studies show that two copies of GCYC2 (GCYC2A/2B) are also found in the Asian genera with three staminodes, such as Chirita  and Opithandra in this study (Figure 2B). The derived morphology of diandrous flowers might have resulted from subsequent expression differentiation after gene duplication events. In the diandrous flowers of Chirita (also Gesneriaceae) that differs from Opithandra in abortion of both the dorsal and lateral stamens rather than ventral stamens, ChCYC1C is strongly expressed both in the dorsal and lateral stamens while ChCYC1D maintains strong expressions in the dorsal floral regions, and ChCYC2A/2B have no expression signals in floral tissues . No expression of GCYC2 detected in floral tissue is frequently found in Gesneriaceae while GCYC1 is usually conserved in dorsal-specific expression in this family, such as Oreocharis and Bournea [35, 39]. Therefore, the peculiar diandrous flowers established in Opithandra might involved not only gained or enhanced expression of OpdCYC1C in ventral staminodes but also the reactivated expression of OpdCYC2A specific to the dorsal staminode accompanied with the downregulation of OpdCYC1D in the dorsal region in the third whorl, a more complicated mechanism than that in another diandrous flowers of Chirita.
Phylogenetic analyses show that the CYC-like genes isolated from Opithandra and other Gesneriaceae belong to ECE-CYC2 clade as CYC and TCP1 from Antirrhinum and Arabidopsis (Figure 2B) [25, 35, 39, 45]. As outlined above, ECE-CYC2 clade genes are characteristic of dorsal identity function which sometimes expands to lateral stamens [4, 5, 21, 23, 25, 35, 39]. It would be especially interesting to know whether or how CYC-like gene activities are related to abortion of the ventral stamens [3, 12, 20]. Even though not tested functionally, this positive correlation between CYC-like gene expression and ventral stamen abortion and the complement of cyclinD3 to CYC-like gene expressions suggests a genetic mechanism underlying the establishment of zygomorphy with abortion of both the dorsal and ventral stamen evolved within Lamiales s.l.. However, it has been shown for Veronica and Gratiola (also Lamiales s.l.) that the CYC-like gene expression does not positively correlate with the ventral stamen abortion (Preston et al., 2009). These facts inconsonant in the expression data of ECE-CYC2 clade TCP genes imply that the ventral stamen abortion might have evolved by convergent genetic mechanisms in different lineages of Lamiales s.l.. It merits further research in function and upstream regulatory pathway to determine how the expression divergence is caused among paralogues of OpdCYC in Opithandra. In addition, since the diverse variations of zygomorphy in Lamiales s.l. might have involved independent shifts in stamen number [3, 21], further investigation of expression pattern and functional analyses of CYC-like genes with identification of their upstream cis- or trans-regulators as well as research in finding other factors possibly coopted to this regulatory pathway in more zygomorphic groups would shed new lights on the mechanisms that underlie the vast morphological diversity of zygomorphy in Lamiales s.l..
As the first to document the expression domain of ECE-CYC clade genes in the ventral stamens, we here report that the expressions of OpdCYC genes are correlated with abortion of both dorsal and ventral stamens in Opithandra, strengthened by the negatively correlated expression of their putative direct target OpdcyclinD3 genes. The complement of OpdcyclinD3 to OpdCYC gene expressions further indicates that OpdCYC expressions are related to the dorsal and ventral stamen abortion through the negative effect on OpdcyclinD3 genes. The novel patterns of CYC-like gene expressions in Opithandra, along with previous reports, suggest that ECE-CYC2 clade TCP genes are not only functionally conserved in the dorsal stamen repression, but also involved in arresting ventral stamens, a genetic mechanism underlying the establishment of zygomorphy with abortion of both the dorsal and ventral stamens evolved within Lamiales s.l.. It would be important to further find whether ECE-CYC2 clade TCP genes are recruited repeatedly for arresting ventral stamens and (or) whether there is any other genetic pathways underlying the ventral stamen abortion, independently or interacting with ECE-CYC2 clade TCP genes, in different lineages of Lamiales s.l..
All materials used in this study, including gene cloning, in situ hybridization and RT-PCR, were collected from the wild fields, i.e. Dinghu Mountains, Guangdong province, China, where plants of Opithandra dinghushanensis W. T. Wang are mainly distributed.
Gene cloning and sequence analyses
CYC-like genes were isolated from O.dinghushanensis using degenerate oligonucleotide primers in 3' and 5'-RACE according to described methods  and the manufacture's protocol (INVITROGEN), respectively. Two D3-type cyclin genes were also isolated from O. dinghushanensis using the above methods. Total RNA was extracted from the floral buds of O. dinghushanensis using the Plant RNA Purification Reagent (INVITROGEN) according to the manufacture's protocol. First-strand cDNAs were synthesized from total RNA with the Supertranscript™ III RNase H- Reverse Transcriptase (INVITROGEN). To examine the intron/exon structures we isolated and sequenced the corresponding genomic DNA of OpdCYC and OpdcyclinD3 genes from leaves. The Oligonucleotide sequences for primers are included in the Additional Material - Additional file 2.
According to the known sequence information, phylogenetic analyses of CYC-like and D-type cyclin genes were conducted to identify the position of CYC-like and D3-type cyclin genes isolated herein in their gene families, respectively. AmCYC and AmDICH are from A. majus [4, 5], and LjCYC1/2/3, TCP1/12/18 and TB1 are from Lotus japonicus , Arabidopsis  and maize . GCYC1A/1B are from Saintpaulia ionantha and Streptocarpus primulifolius [43–45]. GCYC1C/1D (designated as GCYC1 respectively in some taxa) are from Chirita heterotricha , Jankaea heldeichii , Conandron ramondioides, Haberlea ferdinandi-coburgii, Primulina tabacum, Ramonda myconi , Cyrtandra apiculata, Didymocarpus citrinus and Loxostigma sp. . GCYC2 (2A/2B) are from Chirita heterotricha , Conandron ramondioides, Haberlea ferdinandi-coburgii, Ramonda myconi , Cyrtandra apiculata  and Didymocarpus citrinus (Yin-Zheng Wang, unpublished). Amino acid sequences of D-type cyclin genes are from A. majus (Amcyclin D1/D3a/D3b) , Populus trichocarpa (Ptcyclin D1/D2/D3) , Nicotiana tabacum (Ntcyclin D/D3) , Solanum tuberosum (Stcyclin D) (accession nos.EU325650), Lycopersicon esculentum (Lecyclin D3-1)  and Arabidopsis (Atcyclin D1/D2/D3) . Phylogenetic analyses with the neighbor joining method and p-distance were carried out using PAUP*4.0b4a  and bootstrap was estimated with 1,000 resampling replicates. The DNA sequences of genes reported in this paper, i.e. OpdCYC1C, OpdCYC1D, OpdCYC2A, OpdCYC2B, OpdcyclinD3a and OpdcyclinD3b have been deposited in the GenBank database (accession nos. FJ710518, FJ710519, FJ710520, FJ710521, FJ710522 and FJ644637).
RNA in situ hybridization
Floral tissue for in situ hybridization was fixed, sectioned and hybridized to digoxygenin-labeled probes of OpdCYC1C, OpdCYC1D, OpdCYC2A and OpdCYC2B with reference to described methods . Four gene-specific fragments of OpdCYC1C, OpdCYC1D, OpdCYC2A and OpdCYC2B in the coding region were amplified, respectively, and then were purified and cloned into pGEM®-T Easy vectors. Digoxygenin-labeled probes of OpdCYC1C, OpdCYC1D, OpdCYC2A and OpdCYC2B were prepared from linearized templates amplified using primer Yt7 and Ysp6 from pGEM®-T plasmids . The oligonucleotide sequences for primers are included in the Additional Material - Additional file 2.
Gene-specific semiquantitative RT-PCR
Flowers of different stages were collected as follows: Flower buds of middle-stage (less than 1 cm long) and flowers of late-stage (3-4 cm long) were collected separately. Sepals were removed from the outer whorl. The petals with corresponding corolla-tube were dissected into dorsal (including the attached dorsal staminode), lateral, and ventral regions. Lateral stamens and ventral staminodes were dissected from the corolla-tube and collected each for RT-PCR. All materials were frozen in liquid nitrogen immediately after collection for ribonucleic acid (RNA) isolation. The extraction of total RNAs, purification of poly (A) mRNAs, and synthesis of the first-strand cDNAs were performed according to the methods described above. The template quantity was regulated to be uniform using the ACTIN gene . PCR was performed by using gene-specific primers of OpdCYC1C, OpdCYC1D, OpdCYC2A, OpdCYC2B, OpdcyclinD3a and OpdcyclinD3b. To make sure that each pair of primers was suitable, we first used them to amplify genomic DNA of O. dinghushanensis. The PCR products were then cloned. At least 20 clones of each PCR product were sequenced, and all the primers used could amplify the specific copies of OpdCYC and OpdcyclinD3 genes. The following thermocycling conditions were employed: initial denaturation at 96°C for 3 min, 30 cycles of 96°C for 30 s, 55-60°C (depending on the Tm value of primer pairs) for 30s, and 72°C for 1 min, and a final extension at 72°C for 10 min. The amplified products were separated on a 1.5% agarose gel, and the density of ethidium bromide-stained bands was determined using a Bioimaging System (Gene Tools Program, Syngene, UK). We repeated the RT-PCR experiments five times independently with a new RNA extraction each time. In addition, all RT-PCR products were cloned into pGEM-T Easy-vector, and at least 20 clones from each product were sequenced to test the gene specificity of RT-PCR. The OpdCYC/ACTIN and Opdcyclin/ACTIN ratios represented the relative level of OpdCYC and OpdcyclinD3 mRNA expression. Data are presented as the mean ± SD of independent RT-PCR experiments, and one-way analysis of variance was used to analyze the expression difference of these transcripts in floral tissue from O. dinghushanensis. A P value less than 0.05 was taken to indicate statistical significance. The oligonucleotide sequences for primers are included in the Additional Material - Additional file 2.
We thank Dr. James Smith for his critical comments and language improvement on the manuscript. This work was supported by CAS Grant KSCX2-YW-R-135 and National Natural Science Foundation of China Grant, no.30770147.
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